1513855-74-7
![N6-[[(4-Azidophenyl)methoxy]carbonyl]-L-lysine Chemical Structure](http://file.medchemexpress.cn/product_pic/hy-154835.gif "N6-[[(4-Azidophenyl)methoxy]carbonyl]-L-lysine Chemical Structure")
Chemical Structure
N6-[[(4-Azidophenyl)methoxy]carbonyl]-L-lysine
- CAS No.: 1513855-74-7
- Formula:C14H19N5O4
- Molecular Weight:321.33
IUPAC Name: N6-(((4-azidobenzyl)oxy)carbonyl)-L-lysine
InChIKey: TZQHUQASIQQHCK-LBPRGKRZSA-N
SMILES: N[C@@H](CCCCNC(OCC1=CC=C(N=[N+]=[N-])C=C1)=O)C(O)=O
Biological Activity: N6-[[(4-Azidophenyl)methoxy]carbonyl]-L-lysine is an unnatural amino acid[1]. N6-[[(4-Azidophenyl)methoxy]carbonyl]-L-lysine is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
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N6-[[(4-Azidophenyl)methoxy]carbonyl]-L-lysine | N6-[[(4-Azidophenyl)methoxy]carbonyl]-L-lysine is an unnatural amino acid. N6-[[(4-Azidophenyl)methoxy]carbonyl]-L-lysine is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups. | |||||||||||||||||||||
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